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February 1, 2020Journal of Vascular Diagnostics and InterventionsOpen Access

Endomyocardial Fibrosis: Diagnosis and Management

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Why the study?

Endomyocardial fibrosis is a restrictive cardiomyopathy of unknown etiology that carries high morbidity and mortality, requiring review of its diagnosis and management.

Design

Review

Key result

Endomyocardial fibrosis is a restrictive cardiomyopathy with a poor prognosis, where the duration of illness from presentation to death is less than one year in 43.5% of patients.

Authors

SKSiddiq Ibrahim Khalil

Discussion

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Overview

EMF carries high morbidity/mortality in young African females; leaves open etiology, diagnostics, and optimal therapies.

Structured PICO

P
Population
Patients with Endomyocardial Fibrosis (EMF), predominantly children and young females from poor and deprived communities of tropical Africa and other subtropical countries.
E
Exposure
Medical therapy (diuretics, angiotensin enzyme inhibitors, beta-blockers) and surgical care (pericardectomy, endocardial decortication)

Endomyocardial fibrosis is a restrictive cardiomyopathy of unknown etiology with a poor prognosis, primarily affecting young populations in tropical regions, where echocardiography is the gold standard for diagnosis.

Cite This Study

Siddiq Ibrahim Khalil (2020) conducted a review in Endomyocardial Fibrosis. Endomyocardial fibrosis is a restrictive cardiomyopathy with a poor prognosis, where the duration of illness from presentation to death is less than one year in 43.5% of patients.

synapsesocial.com/papers/6a7a3be9e357fbdac5896c92https://doi.org/10.2147/jvd.s196348
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